View genomic variant #0000022894

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.136219564G>C
Published as -
GERP -
Segregation -
DB-ID SURF1_000031
MSCV MSCV_0022894
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.05422 View details
Owner LOVD




Variant on transcripts

2 entries on 1 page. Showing entries 1 - 2.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
SURF1 00000317 NM_001280787.1 0000022894 ./. - - c.246C>G p.(=) - - - -
SURF1 00000318 NM_003172.3 0000022894 ./. - - c.573C>G p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV003066952;
Chromosome 9:136219564..136219564
ClinVar Allele ID 1876694
Disease database name and identifier MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name Leigh syndrome
HGVS variant names NC 000009.11:g.136219564G>A
ClinVar review status criteria provided, single submitter
Clinical Significance Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. SURF1:6834
Molecular consequence SO:0001819|synonymous variant
Allele origin germline
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000128341; RCV000298807; RCV000676733; RCV002492492;
Chromosome 9:136219564..136219564
Allele frequencies from ESP 0.05422
Allele frequencies from TGP 0.04173
ClinVar Allele ID 143077
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506|MedGen:CN169374|MONDO:MONDO:0009068, MedGen:C5435656, OMIM:220110, Orphanet:254905|MONDO:MONDO:0014733, MedGen:C4225246, OMIM:616684, Orphanet:391351
ClinVar preferred disease name not provided|Leigh syndrome|not specified|Cytochrome-c oxidase deficiency disease|Charcot-Marie-Tooth disease type 4K
HGVS variant names NC 000009.11:g.136219564G>C
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign/Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA293827
Gene symbol:Gene id. SURF1:6834
Molecular consequence SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 28715079
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None